UA77010C2 - Гербіцидний засіб на основі заміщених тієн-3-іл-сульфоніламіно(тіо)карбонілтриазолін(ті)онів і сафенерів - Google Patents

Гербіцидний засіб на основі заміщених тієн-3-іл-сульфоніламіно(тіо)карбонілтриазолін(ті)онів і сафенерів Download PDF

Info

Publication number: UA77010C2
Authority: UA; Ukraine
Prior art keywords: substituted; necessary; fluorine; chlorine; cyano
Prior art date: 2001-09-21

Application number

UA20040402902A

Other languages

English (en)

Russian (ru)

Ukrainian (uk)

Inventor

Дітер Фойхт

Дитер Фойхт

Петер Дамен

Марк Вільхельм Древес

Марк Вильхельм Древес

Рольф Понтцен

Ернст Рудольф Ф. Гезінг

Ханс-Георг Шварц

Клаус-Хельмут Мюллер

Original Assignee

Баєр Кропсаєнс Аг

Байер Кропсайенс

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2001-09-21

Filing date

2002-10-09

Publication date

2006-10-16

2002-10-09 Application filed by Баєр Кропсаєнс Аг, Байер Кропсайенс filed Critical Баєр Кропсаєнс Аг

2006-10-16 Publication of UA77010C2 publication Critical patent/UA77010C2/uk

Links

239000004009 herbicide Substances 0.000 title abstract description 10
150000001875 compounds Chemical class 0.000 abstract description 54
239000003795 chemical substances by application Substances 0.000 abstract description 6
150000003839 salts Chemical class 0.000 abstract description 6
239000004480 active ingredient Substances 0.000 abstract 1
238000004519 manufacturing process Methods 0.000 abstract 1
230000008635 plant growth Effects 0.000 abstract 1
-1 hydroxy, mercapto, amino Chemical group 0.000 description 236
239000000460 chlorine Substances 0.000 description 119
229910052801 chlorine Inorganic materials 0.000 description 119
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 111
239000011737 fluorine Substances 0.000 description 85
229910052731 fluorine Inorganic materials 0.000 description 85
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 74
229910052794 bromium Inorganic materials 0.000 description 74
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 74
125000001153 fluoro group Chemical group F* 0.000 description 68
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 66
229910052739 hydrogen Inorganic materials 0.000 description 62
239000001257 hydrogen Substances 0.000 description 61
150000002431 hydrogen Chemical class 0.000 description 57
125000004093 cyano group Chemical group *C#N 0.000 description 55
239000000126 substance Substances 0.000 description 54
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239000013543 active substance Substances 0.000 description 43
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230000006378 damage Effects 0.000 description 28
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238000011160 research Methods 0.000 description 23
239000002253 acid Substances 0.000 description 19
210000000988 bone and bone Anatomy 0.000 description 18
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125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 6
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239000000843 powder Substances 0.000 description 6
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125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 5
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239000008187 granular material Substances 0.000 description 5
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230000002363 herbicidal effect Effects 0.000 description 5
238000000034 method Methods 0.000 description 5
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239000012895 dilution Substances 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
REVLCBCMFHHOGK-UHFFFAOYSA-N ethyl 4,5-dihydro-1,2-oxazole-3-carboxylate Chemical compound CCOC(=O)C1=NOCC1 REVLCBCMFHHOGK-UHFFFAOYSA-N 0.000 description 1
SQFPMCDRPGJOQH-UHFFFAOYSA-N ethyl 5-(4-fluorophenyl)-5-phenyl-4h-1,2-oxazole-3-carboxylate Chemical compound C1C(C(=O)OCC)=NOC1(C=1C=CC(F)=CC=1)C1=CC=CC=C1 SQFPMCDRPGJOQH-UHFFFAOYSA-N 0.000 description 1
125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical group C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
159000000003 magnesium salts Chemical class 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000002207 metabolite Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
RMIODHQZRUFFFF-UHFFFAOYSA-N methoxyacetic acid Chemical compound COCC(O)=O RMIODHQZRUFFFF-UHFFFAOYSA-N 0.000 description 1
IZYBEMGNIUSSAX-UHFFFAOYSA-N methyl benzenecarboperoxoate Chemical compound COOC(=O)C1=CC=CC=C1 IZYBEMGNIUSSAX-UHFFFAOYSA-N 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000006431 methyl cyclopropyl group Chemical group 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 1
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 description 1
229940042880 natural phospholipid Drugs 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
229960003512 nicotinic acid Drugs 0.000 description 1
235000016709 nutrition Nutrition 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
125000003566 oxetanyl group Chemical group 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
HFGGXBQZQRVOKM-UHFFFAOYSA-N piperidine-1-carbothioic s-acid Chemical compound SC(=O)N1CCCCC1 HFGGXBQZQRVOKM-UHFFFAOYSA-N 0.000 description 1
230000001863 plant nutrition Effects 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000015277 pork Nutrition 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
TURAMGVWNUTQKH-UHFFFAOYSA-N propa-1,2-dien-1-one Chemical group C=C=C=O TURAMGVWNUTQKH-UHFFFAOYSA-N 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
125000006320 propynyl amino group Chemical group 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
235000015136 pumpkin Nutrition 0.000 description 1
239000010453 quartz Substances 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
229910052703 rhodium Inorganic materials 0.000 description 1
239000010948 rhodium Substances 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
230000005070 ripening Effects 0.000 description 1
239000011435 rock Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
230000000392 somatic effect Effects 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
125000004646 sulfenyl group Chemical group S(*)* 0.000 description 1
125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000012360 testing method Methods 0.000 description 1
125000005958 tetrahydrothienyl group Chemical group 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
230000001256 tonic effect Effects 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
CTMHWPIWNRWQEG-UHFFFAOYSA-N trans cyclohexenyl ester Natural products CC1=CCCCC1 CTMHWPIWNRWQEG-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical group 0.000 description 1
210000002700 urine Anatomy 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

UA20040402902A 2001-09-21 2002-10-09 Гербіцидний засіб на основі заміщених тієн-3-іл-сульфоніламіно(тіо)карбонілтриазолін(ті)онів і сафенерів UA77010C2 (uk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE10146590A DE10146590A1 (de)	2001-09-21	2001-09-21	Selektive Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen und Safenern
PCT/EP2002/010104 WO2003026427A1 (de)	2001-09-21	2002-09-10	Selektive herbizide auf basis von substituierten thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen und safenern

Publications (1)

Publication Number	Publication Date
UA77010C2 true UA77010C2 (uk)	2006-10-16

Family

ID=7699812

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA20040402902A UA77010C2 (uk)	2001-09-21	2002-10-09	Гербіцидний засіб на основі заміщених тієн-3-іл-сульфоніламіно(тіо)карбонілтриазолін(ті)онів і сафенерів

Country Status (24)

Country	Link
US (4)	US20050009705A1 (hu)
EP (1)	EP1429613B1 (hu)
JP (2)	JP4610895B2 (hu)
KR (2)	KR100927025B1 (hu)
CN (1)	CN1326457C (hu)
AR (1)	AR036775A1 (hu)
AU (1)	AU2002333811B8 (hu)
BE (2)	BE2016C043I2 (hu)
CA (2)	CA2695675C (hu)
CO (1)	CO5580725A2 (hu)
DE (2)	DE10146590A1 (hu)
ES (1)	ES2280615T3 (hu)
FR (2)	FR17C1034I2 (hu)
HR (1)	HRP20040359A2 (hu)
HU (3)	HU230218B1 (hu)
MX (1)	MXPA04002641A (hu)
NL (3)	NL350074I2 (hu)
PL (1)	PL207754B1 (hu)
PT (1)	PT1429613E (hu)
RS (1)	RS51046B (hu)
RU (1)	RU2308834C2 (hu)
UA (1)	UA77010C2 (hu)
WO (1)	WO2003026427A1 (hu)
ZA (1)	ZA200402129B (hu)

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DE10146591A1 (de) *	2001-09-21	2003-04-10	Bayer Cropscience Ag	Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen
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DE10031825A1 (de) *	2000-06-30	2002-01-10	Bayer Ag	Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen
DE10146590A1 (de) *	2001-09-21	2003-04-10	Bayer Cropscience Ag	Selektive Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen und Safenern
DE10146591A1 (de) *	2001-09-21	2003-04-10	Bayer Cropscience Ag	Herbizide auf Basis von substituierten Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)onen

2001
- 2001-09-21 DE DE10146590A patent/DE10146590A1/de not_active Withdrawn
2002
- 2002-08-30 AR ARP020103292A patent/AR036775A1/es active IP Right Grant
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- 2002-09-10 WO PCT/EP2002/010104 patent/WO2003026427A1/de active Application Filing
- 2002-09-10 KR KR1020047003225A patent/KR100927025B1/ko active IP Right Grant
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- 2002-09-10 RU RU2004112214/04A patent/RU2308834C2/ru active Protection Beyond IP Right Term
- 2002-09-10 KR KR1020097019065A patent/KR100979997B1/ko active IP Right Grant
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- 2002-10-09 UA UA20040402902A patent/UA77010C2/uk unknown
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2009
- 2009-12-22 JP JP2009290184A patent/JP2010100638A/ja active Pending
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- 2013-04-30 US US13/873,656 patent/US9968091B2/en not_active Expired - Lifetime
2015
- 2015-11-24 US US14/950,588 patent/US10524475B2/en not_active Expired - Lifetime
2016
- 2016-01-21 HU HUS1600007C patent/HUS1600007I1/hu unknown
- 2016-08-05 NL NL350074C patent/NL350074I2/nl unknown
- 2016-08-18 BE BE2016C043C patent/BE2016C043I2/fr unknown
2017
- 2017-02-02 NL NL350078C patent/NL350078I2/nl unknown
- 2017-09-20 FR FR17C1034C patent/FR17C1034I2/fr active Active
- 2017-11-15 BE BE2017C050C patent/BE2017C050I2/fr unknown
- 2017-12-07 NL NL350082C patent/NL350082I2/nl unknown
2018
- 2018-04-20 FR FR18C1015C patent/FR18C1015I2/fr active Active
2019
- 2019-11-21 US US16/690,200 patent/US20200085058A1/en not_active Abandoned
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Also Published As

Publication number	Publication date
FR18C1015I1 (hu)	2018-06-15
HUP0402116A2 (hu)	2005-01-28
CO5580725A2 (es)	2005-11-30
HUS2000029I1 (hu)	2021-03-29
AU2002333811B8 (en)	2008-09-11
CN1326457C (zh)	2007-07-18
FR17C1034I2 (fr)	2019-08-09
HUS1600007I1 (hu)	2018-11-28
HRP20040359A2 (en)	2005-04-30
DE50209305D1 (de)	2007-03-08
US10524475B2 (en)	2020-01-07
KR100927025B1 (ko)	2009-11-19
EP1429613B1 (de)	2007-01-17
KR20090105978A (ko)	2009-10-07
US20200085058A1 (en)	2020-03-19
KR20040053119A (ko)	2004-06-23
MXPA04002641A (es)	2004-06-07
EP1429613A1 (de)	2004-06-23
PT1429613E (pt)	2007-03-30
NL350078I2 (nl)	2017-07-11
WO2003026427A1 (de)	2003-04-03
FR18C1015I2 (fr)	2019-06-21
CN1555221A (zh)	2004-12-15
HUS000505I2 (hu)	2021-03-29
JP2005503421A (ja)	2005-02-03
HUP0402116A3 (en)	2005-10-28
RS24504A (en)	2006-12-15
CA2460922A1 (en)	2003-04-03
JP2010100638A (ja)	2010-05-06
CA2695675A1 (en)	2003-04-03
BE2016C043I2 (hu)	2021-07-19
ZA200402129B (en)	2005-06-29
JP4610895B2 (ja)	2011-01-12
US9968091B2 (en)	2018-05-15
RS51046B (sr)	2010-10-31
HU230218B1 (hu)	2015-10-28
US20130237418A1 (en)	2013-09-12
NL350078I1 (nl)	2017-02-08
PL207754B1 (pl)	2011-01-31
AU2002333811B2 (en)	2008-08-14
FR17C1034I1 (hu)	2017-10-27
BE2017C050I2 (hu)	2021-11-22
US20160073635A1 (en)	2016-03-17
NL350074I2 (hu)	2016-09-01
NL350082I2 (nl)	2018-01-24
AR036775A1 (es)	2004-10-06
CA2695675C (en)	2013-04-23
RU2004112214A (ru)	2005-10-10
KR100979997B1 (ko)	2010-09-03
HRP20040359B1 (hu)	2012-11-30
PL367511A1 (en)	2005-02-21
RU2308834C2 (ru)	2007-10-27
ES2280615T3 (es)	2007-09-16
CA2460922C (en)	2011-07-05
US20050009705A1 (en)	2005-01-13
DE10146590A1 (de)	2003-04-10

Publication	Publication Date	Title
UA77010C2 (uk)	2006-10-16	Гербіцидний засіб на основі заміщених тієн-3-іл-сульфоніламіно(тіо)карбонілтриазолін(ті)онів і сафенерів
EP0432600A2 (de)	1991-06-19	2-Iminopyridin-Derivate
JPS58124773A (ja)	1983-07-25	５−メチルチオピリミジン誘導体とその製造法と農園芸用殺菌剤
DE4437049A1 (de)	1996-04-18	Selektive Herbizide auf Basis von Carbamoyltriazolinonen und Heteroaryloxyacetamiden
EP0274642A2 (de)	1988-07-20	Herbizide und fungizide Mittel auf Basis von substituierten Pyrazolin-5-on-Derivaten
EP1049376A1 (de)	2000-11-08	Selektive herbizide auf basis von n-aryl-triazolin(thi)onen und n-arylsulfonylamino(thio)carbonyl-triazolin(thi)onen
EP0298371B1 (de)	1991-10-02	Substituierte Triazolinone
KR20040111382A (ko)	2004-12-31	환상 화합물, 이의 제조 방법 및 그를 사용하는 해충방제제
EP0355385B1 (de)	1993-05-19	Substituierte 4-Sulfonylamino-2-azinyl-1,2,4-triazol-3-one, Verfahren sowie Zwischenprodukte zu ihrer Herstellung und ihre Verwendung als Herbizide
DE3004326A1 (de)	1981-08-13	Azolyloxy-carbonsaeureamide, verfahren zu ihrer herstellung un ihre verwendung als herbinzide
EP0399294B1 (de)	1994-02-02	Substituierte Triazolinone
EP0467183A1 (de)	1992-01-22	Herbizide auf Basis von sulfonylierten (Thio)Carbamidsäureestern, neue sulfonylierte Carbamidsäureester und Verfahren zu deren Herstellung
DE3916208A1 (de)	1990-11-22	Substituierte triazolone
WO1982000402A1 (en)	1982-02-18	Herbicidal and plant growth regulant diphenylpyridazinones
HU230521B1 (hu)	2016-10-28	Heteroariloxi-acetamid-származékot tartalmazó szelektív herbicid készítmények
EP0433749A2 (de)	1991-06-26	Pyrazolin-5-on-Derivate
JP2004529094A (ja)	2004-09-24	置換アリールケトン及び薬害軽減剤に基づく選択的除草剤
EP1427699B1 (de)	2011-08-03	Selektive herbizide auf basis von substituierten arylsulfonylaminocarbonyltriazolinonen und safenern
EP0431270A1 (de)	1991-06-12	Substituierte Sulfonylamidinohydrazone
DE4112329A1 (de)	1992-10-22	Cyanothiazolderivate
DE4021658A1 (de)	1992-01-09	2-acylamino-7-chlorbenzthiazole
EP0467139A2 (de)	1992-01-22	Nicotinsäurederivate als Herbizide
EP0282811A1 (de)	1988-09-21	4-Cyano-1-aryl-pyrazole
EP0067981A2 (de)	1982-12-29	Neue Pyrazol-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide
DE3920414A1 (de)	1991-01-03	Halogen-triazolone